Influence of exogenous application of proline and glycinebetaine on growth of salt-stressed tomato plants

By B. Heuer. 2003

221 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/b26c3d0a37421298a07d41d4f8eb908b8e9e9ae1

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In Plant Science

Citations in the corpus

Exogenous Glycine Betaine Ameliorates the Adverse Effect of Salt Stress on Perennial Ryegrass (2012, background): “A higher level of proline accumulation resulting from GB application under salinity has been found in rice (Demiral and Türkan, 2006) and tomato (Heuer, 2003).”
Glycine betaine: a versatile compound with great potential for gene pyramiding to improve crop plant performance against environmental stresses (2012, background): “Although, an overwhelming number of studies depicts positive effects of GB on plants, there are a few reports which show that GB can exert negative effects when exogenously applied to naturally non-GB accumulators (Heuer 2003; Larher et al. 1996; Sulpice et al. 1998).”
Ascophyllum nodosum-based algal extracts act as enhancers of growth, fruit quality, and adaptation to stress in salinized tomato plants (2018, background): “This was also observed in previous experiments with exogenous applications of proline in tomato plants (Heuer 2003).”
Effects of Salt and Water Stress on Plant Growth and on Accumulation of Osmolytes and Antioxidant Compounds in Cherry Tomato (2015, background): “Nevertheless, exogenous application of GB to tomato plants improves their resistance to drought (Rezaei et al., 2012) and salinity (Chen et al., 2009; Heuer, 2003; Makela et al., 1998).”
Water Relation, Photosynthetic Ability and Growth of Thai Jasmine Rice (Oryza sativa L. ssp. indica cv. KDML 105) to Salt Stress by Application of Exogenous Glycinebetaine and Choline (2006, background): “2003) and by functioning as oxygen radical scavengers (Heuer 2003).”
Effect of glycinebetaine on proline, water use, and photosynthetic efficiencies, and growth of rice seedlings under salt stress (2010, background): “…in plants exposed to saline soil is probably protecting plant cells from salt stress by osmotic adjustment (Gadallah 1999), protein stabilization (RuBisCo) (Mäkelä et al. 2000), photosynthetic apparatus protection (Allakhverdiev et al. 2003), and reduction of oxygen radical scavengers (Heuer 2003).”
Plant Response to Salt Stress and Role of Exogenous Protectants to Mitigate Salt-Induced Damages (2013, background): “Proline perform these functions by protecting the photosynthetic apparatus (Ashraf et al. 2008 ) , by functioning as an oxygen radical scavenger (Heuer 2003 ) , and by displaying an antioxidant activity (Okuma et al. 2004 ) .”
Effects of seed hydropriming in presence of exogenous proline on chilling injury limitation in Vigna radiata L. seedlings (2007, background): “Although, negative effects, such as troubles in inorganic ions balance in tomato plants (Lycopersicon esculentum) (Heuer 2003) or growth inhibition in suspension cultures of saltgrass (Distichlis spicata) (Rodriquez and Heyser 1988), are also noticed.”
Overcoming Salinity Barriers to Crop Production Using Traditional Methods (2013, methodology): “Reduced accumulation of Na and Cl was also found in tomato plants grown in nutrient solution containing 135 mM NaCl, when 1 or 5 mM GB or 1 mM proline was added to the solution (Heuer, 2003).”
Glycinebetaine accumulation, physiological characterizations and growth efficiency in salt-tolerant and salt-sensitive lines of indica rice (Oryza sativa L. ssp. indica) in response to salt stress (2007, background): “2003) and (iv) functioning as radical oxygen scavengers (Heuer 2003), thereby promoting the photosynthetic capacity during salt or drought stress (Agboma et al.”
Roles of glycine betaine in mitigating deleterious effect of salt stress on lettuce (Lactuca sativa L.) (2015, background): “The ameliorative effects of the exogenous application of GB has been reported in inducing salt tolerance in many vegetable crops, including tomato (Mäkela et al. 1998; Heuer 2003), broad bean (Gadallah 1999), eggplant (Abbas et al. 2010) and okra (Habib et al. 2012).”
Metabolic and molecular-genetic regulation of proline signaling and itscross-talk with major effectors mediates abiotic stress tolerance in plants (2015, background): “This was seen when the growth of tomato seedlings under salt stress was inhibited with Pro supplied in the growth medium (Heuer, 2003).”